High performance of systematic combined urine LAM test and sputum Xpert MTB/RIF® for tuberculosis screening in severely immunosuppressed ambulatory adults with HIV.

HIV diagnosis screening tuberculosis

Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
08 Mar 2023
Historique:
received: 21 11 2022
revised: 10 02 2023
accepted: 02 03 2023
entrez: 8 3 2023
pubmed: 9 3 2023
medline: 9 3 2023
Statut: aheadofprint

Résumé

In people with HIV (PWH), the WHO-recommended tuberculosis four-symptom screen (W4SS) targeting those who need molecular rapid test may be suboptimal. We assessed the performance of different tuberculosis screening approaches in severely immunosuppressed PWH enrolled in the guided-treatment group of the STATIS trial (NCT02057796). Ambulatory PWH with no overt evidence of tuberculosis and CD4 cell count <100/µL were screened for tuberculosis prior to antiretroviral therapy (ART) initiation with W4SS, chest X-ray, urine lipoarabinomannan (LAM) test and sputum Xpert MTB/RIF® (Xpert). Correctly and wrongly identified cases by screening approaches were assessed overall and by CD4 count threshold (≤50 and 51-99 cells/µL). Of 525 enrolled participants (median CD4 cell count: 28/µL), 48 (9.9%) were diagnosed with tuberculosis at enrollment. Among participants with a negative W4SS, 16% had either a positive Xpert, a chest X-ray suggestive of tuberculosis or a positive urine LAM test. The combination of sputum Xpert and urine LAM test was associated with the highest proportion of participants correctly identified as tuberculosis (95.8%) and non-tuberculosis cases (95.4%), with proportions equally high among participants with CD4 counts above or below 50 cells/µL. Restricting the use of sputum Xpert, urine LAM test or chest X-ray to participants with a positive W4SS reduced the proportion of wrongly and correctly identified cases. There is a clear benefit to perform both sputum Xpert and urine LAM tests as tuberculosis screening in all severely immunosuppressed PWH prior to ART initiation, and not only in those with a positive W4SS. NCT02057796.

Sections du résumé

BACKGROUND BACKGROUND
In people with HIV (PWH), the WHO-recommended tuberculosis four-symptom screen (W4SS) targeting those who need molecular rapid test may be suboptimal. We assessed the performance of different tuberculosis screening approaches in severely immunosuppressed PWH enrolled in the guided-treatment group of the STATIS trial (NCT02057796).
METHODS METHODS
Ambulatory PWH with no overt evidence of tuberculosis and CD4 cell count <100/µL were screened for tuberculosis prior to antiretroviral therapy (ART) initiation with W4SS, chest X-ray, urine lipoarabinomannan (LAM) test and sputum Xpert MTB/RIF® (Xpert). Correctly and wrongly identified cases by screening approaches were assessed overall and by CD4 count threshold (≤50 and 51-99 cells/µL).
RESULTS RESULTS
Of 525 enrolled participants (median CD4 cell count: 28/µL), 48 (9.9%) were diagnosed with tuberculosis at enrollment. Among participants with a negative W4SS, 16% had either a positive Xpert, a chest X-ray suggestive of tuberculosis or a positive urine LAM test. The combination of sputum Xpert and urine LAM test was associated with the highest proportion of participants correctly identified as tuberculosis (95.8%) and non-tuberculosis cases (95.4%), with proportions equally high among participants with CD4 counts above or below 50 cells/µL. Restricting the use of sputum Xpert, urine LAM test or chest X-ray to participants with a positive W4SS reduced the proportion of wrongly and correctly identified cases.
CONCLUSIONS CONCLUSIONS
There is a clear benefit to perform both sputum Xpert and urine LAM tests as tuberculosis screening in all severely immunosuppressed PWH prior to ART initiation, and not only in those with a positive W4SS.
CLINICAL TRIALS REGISTRATION BACKGROUND
NCT02057796.

Identifiants

pubmed: 36883573
pii: 7072300
doi: 10.1093/cid/ciad125
pii:
doi:

Banques de données

ClinicalTrials.gov
['NCT02057796']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Maryline Bonnet (M)

University of Montpellier, IRD, INSERM, TransVIHMI, Montpellier, France.

Delphine Gabillard (D)

University of Bordeaux, INSERM, IRD, Bordeaux, France.

Serge Domoua (S)

Félix Houphouët-Boigny University, Abidjan, Côte d'Ivoire.

Conrad Muzoora (C)

Mbarara University of Science and Technology, Mbarara, Uganda.

Eugène Messou (E)

PAC-CI, Abidjan, Côte d'Ivoire.

Samreth Sovannarith (S)

National Centre for HIV/AIDS, Dermatology and STDs, Phnom Penh, Cambodia.

Duc Bang Nguyen (DB)

Pham Ngoc Thach Hospital, Ho Chi Minh City, Vietnam.

Anani Badje (A)

University of Bordeaux, INSERM, IRD, Bordeaux, France.
PAC-CI, Abidjan, Côte d'Ivoire.

Sylvain Juchet (S)

PAC-CI, Abidjan, Côte d'Ivoire.

Dim Bunnet (D)

Institut Pasteur du Cambodge, Phnom Penh, Cambodia.

Laurence Borand (L)

Institut Pasteur du Cambodge, Phnom Penh, Cambodia.

Naome Natukunda (N)

Epicentre, Mbarara, Uganda.

Thị Hong Tran (TH)

Pham Ngoc Thach Hospital, Ho Chi Minh City, Vietnam.

Xavier Anglaret (X)

University of Bordeaux, INSERM, IRD, Bordeaux, France.

Didier Laureillard (D)

Department of Infectious and Tropical Diseases, University Hospital, Nîmes, France.
Research unit "Pathogenesis and Control of Chronical and Emerging Infections", INSERM, French Blood Center, University of Montpellier, Montpellier, France.

François-Xavier Blanc (FX)

Nantes Université, CHU Nantes, Service de Pneumologie, L'Institut du thorax, Nantes, France.

Classifications MeSH